Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 15, 2026, FDA's public records list Neotech Products with 6 510(k) clearances. The most recent is a 510(k) clearance dated Jan 3, 2002: NEOLEAD.
| Jan 3, 2002 | NEOLEADK011564 · DRX | 510(k) clearances |
| Jul 23, 1993 | URINARY DRAINAGE BAG CADDYK931727 · FAQ | 510(k) clearances |
| Sep 2, 1992 | URO-TOTE LEG BAGK921024 · KNX | 510(k) clearances |
| Apr 19, 1989 | NEOTECH MUCUS TRAP W/CATHETERK890425 · BSY | 510(k) clearances |
| Jun 17, 1988 | NEOTECH UNIVERSAL ADAPTERK882203 · BZA | 510(k) clearances |
| May 6, 1988 | NEOTECH MECONIUM ASPIRATOR (STERILE)K880487 · BTR | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
